C92006
吲哚-5-甲腈
99%
别名:
5-Cyanoindole
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关于此项目
经验公式（希尔记法）:
C9H6N2
化学文摘社编号:
分子量:
142.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
239-986-4
Beilstein/REAXYS Number:
116738
MDL number:
Assay:
99%
Form:
powder
InChI
1S/C9H6N2/c10-6-7-1-2-9-8(5-7)3-4-11-9/h1-5,11H
InChI key
YHYLDEVWYOFIJK-UHFFFAOYSA-N
SMILES string
N#Cc1ccc2[nH]ccc2c1
assay
99%
form
powder
Quality Level
Application
- Reactant for parallel synthesis of dihydroisoquinolines via silver and L-proline co-catalyzed three-component coupling reaction
- Reactant for chemoselective and regioselective preparation of benzoyl indoles
- Reactant for preparation of novel PPARα/γ dual agonists for potential treatment of metabolic syndrome and IDDM
- Reactant for preparation of 4,5-dihydrocyclopenta[c]quinolines by palladium-catalyzed ring-expansion reaction alkynes, using O2 as the oxidant
- Reactant for preparation of vinylindoles by hydroarylation of alkynes using indium bromide catalyst
- Reactant for gold catalyzed direct alkynylation using a benziodoxolone based hypervalent iodine reagent
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Josefin Wilke et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 17(17), 2736-2743 (2016-06-02)
The estimate of the magnitude and the orientation of molecular electric dipole moments from the vector sum of bond or fragment dipole moments is a widely used approach in chemistry. However, the limitations of this intuitive model have rarely been
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